Canonical Allele Identifier: CA366388947

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634466
• MyVariant Identifiers: chr6:g.157469919C>T (hg19) ; chr6:g.157148785C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148785C>T , CM000668.2:g.157148785C>T	GRCh38
NC_000006.11:g.157469919C>T , CM000668.1:g.157469919C>T	GRCh37
NC_000006.10:g.157511611C>T	NCBI36
NG_032093.1:g.375856C>T
NG_032093.2:g.375856C>T
NG_066624.1:g.377760C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2923C>T	ENSP00000055163.8:p.Gln975Ter
ENST00000414678.8:c.2833C>T	ENSP00000412835.3:p.Gln945Ter
ENST00000637015.2:c.2923C>T	ENSP00000489729.2:p.Gln975Ter
ENST00000319584.11:c.937C>T	ENSP00000313006.7:p.Gln313Ter
ENST00000346085.10:c.2962C>T	ENSP00000344546.5:p.Gln988Ter
ENST00000350026.10:c.2674C>T	ENSP00000055163.7:p.Gln892Ter
ENST00000414678.7:c.1081C>T	ENSP00000412835.2:p.Gln361Ter
ENST00000452544.2:n.824C>T
ENST00000635849.1:c.244C>T	ENSP00000490948.1:p.Gln82Ter
ENST00000636426.1:n.57C>T
ENST00000636930.2:c.2923C>T MANE Select	ENSP00000490491.2:p.Gln975Ter
ENST00000637015.1:c.162C>T
ENST00000637810.1:c.424C>T	ENSP00000489636.1:p.Gln142Ter
ENST00000637904.1:c.424C>T	ENSP00000490550.1:p.Gln142Ter
ENST00000647938.1:c.2713C>T	ENSP00000498155.1:p.Gln905Ter
ENST00000674190.1:n.1672C>T
ENST00000319584.10:c.940C>T	ENSP00000313006.6:p.Gln314Ter
ENST00000346085.9:c.2713C>T	ENSP00000344546.4:p.Gln905Ter
ENST00000350026.9:c.2674C>T	ENSP00000055163.7:p.Gln892Ter
ENST00000414678.6:c.1081C>T	ENSP00000412835.2:p.Gln361Ter
ENST00000452544.1:n.770C>T
NM_017519.2:c.2674C>T	NP_059989.2:p.Gln892Ter
NM_020732.3:c.2713C>T	NP_065783.3:p.Gln905Ter
XM_005267069.3:c.2674C>T	XP_005267126.2:p.Gln892Ter
XM_011535984.1:c.1624C>T	XP_011534286.1:p.Gln542Ter
XM_011535985.1:c.1444C>T	XP_011534287.1:p.Gln482Ter
XM_011535986.1:c.1204C>T	XP_011534288.1:p.Gln402Ter
XM_011535987.1:c.823C>T	XP_011534289.1:p.Gln275Ter
XM_011535988.1:c.-20+15578C>T	XP_011534290.1:n.-20+15578C>T
NM_001346813.1:c.2674C>T	NP_001333742.1:p.Gln892Ter
NM_001363725.1:c.424C>T	NP_001350654.1:p.Gln142Ter
XM_011535984.2:c.2755C>T	XP_011534286.2:p.Gln919Ter
XM_011535988.3:c.-20+15578C>T	XP_011534290.1:n.-20+15578C>T
XM_017011103.2:c.2755C>T	XP_016866592.1:p.Gln919Ter
XM_017011104.1:c.2755C>T	XP_016866593.1:p.Gln919Ter
XM_017011105.2:c.2755C>T	XP_016866594.1:p.Gln919Ter
XM_017011106.2:c.2755C>T	XP_016866595.1:p.Gln919Ter
XM_017011107.2:c.2575C>T	XP_016866596.1:p.Gln859Ter
XR_002956289.1:n.2838C>T
NM_001363725.2:c.424C>T	NP_001350654.1:p.Gln142Ter
NM_001371656.1:c.2962C>T	NP_001358585.1:p.Gln988Ter
NM_001374820.1:c.2962C>T	NP_001361749.1:p.Gln988Ter
NM_001374828.1:c.2923C>T MANE Select	NP_001361757.1:p.Gln975Ter
NM_017519.3:c.2923C>T	NP_059989.3:p.Gln975Ter